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- Tasks: Lead global clinical studies in oncology, ensuring efficient delivery and quality.
- Company: Join AstraZeneca, a leader in transformative medicines for complex diseases.
- Benefits: Enjoy remote work, a supportive culture, and opportunities for growth.
- Why this job: Make a real impact on patients' lives while working with cutting-edge science.
- Qualifications: 5+ years in study management, preferably in oncology; degree in medical or biological sciences.
- Other info: Be part of an inclusive team that values diversity and lifelong learning.
The predicted salary is between 48000 - 72000 £ per year.
Title – Global Study Manager
Location – Remote
IR35 Status – Inside
Duration – 12 months
Make a more meaningful impact to patients’ lives around the globe!
Here you’ll have the opportunity to make a meaningful difference to patients’ lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines – for the world’s most complex diseases. Answer unmet medical needs by pioneering the next wave of science, focusing on outcomes and shaping the patient ecosystem.
If your passion is science and you want to be part of a team that makes a bigger impact on patients’ lives, then there’s no better place to be.
The Global Study Manager will work closely with the study operations team and Study Leader who is the overall accountable for the delivery of the study. The GSM supports delivery of early-phase global clinical studies within Oncology R&D from study set-up through maintenance, close-out and study archiving. The GSM works cross-functionally with partners to lead & deliver aspects of the clinical study.
Duties will include:
Lead/contribute to the preparation of study documents.
Maintaining and facilitating interactions with both internal and external functions such as CRO to ensure an efficient study delivery to time, cost and quality objective.
Contributing to the planning and conduct of internal and external meeting such as Investigator’s Meetings.
Ensure supply of investigations product and study materials
Ensure that all study documents in scope of GSM’s responsibilities are complete and verified for quality in the Trial Master File.
Essential Qualifications and Experience:
- University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.
- 5+ years of industry experience in Early Phase study management
- 5+ years of industry experience within oncology (desirable)
- Extensive knowledge of GCP, clinical research regulatory requirements and demonstrated abilities in clinical study management processes and clinical/drug development.
- Demonstrated solid project management skills and knowledge of relevant tools
At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and teamwork. Always committed to lifelong learning, growth and development.
We\’d love to hear from you if you have suitable experience by applying to the role
Study Manager employer: AstraZeneca
Contact Detail:
AstraZeneca Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Study Manager
✨Tip Number 1
Familiarize yourself with the latest trends and developments in oncology research. This will not only enhance your understanding of the field but also allow you to engage in meaningful conversations during interviews.
✨Tip Number 2
Network with professionals in the clinical research community, especially those who have experience in early-phase studies. Attend relevant webinars or conferences to make connections that could lead to valuable insights and opportunities.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences that demonstrate your project management skills and your ability to work cross-functionally. Highlighting these competencies will show that you are well-suited for the Global Study Manager role.
✨Tip Number 4
Research AstraZeneca's culture and values, particularly their commitment to diversity and teamwork. Being able to articulate how your personal values align with theirs can set you apart as a candidate who is not only qualified but also a great cultural fit.
We think you need these skills to ace Study Manager
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Global Study Manager position. Understand the key responsibilities and qualifications required, especially focusing on the aspects related to early-phase global clinical studies and oncology.
Tailor Your CV: Customize your CV to highlight your relevant experience in clinical study management, particularly in early-phase studies and oncology. Emphasize your project management skills and any specific tools you are proficient in that relate to the role.
Craft a Compelling Cover Letter: Write a cover letter that connects your passion for science with the mission of the company. Discuss how your background aligns with the responsibilities of the Global Study Manager and how you can contribute to making a meaningful impact on patients' lives.
Proofread and Submit: Before submitting your application, carefully proofread all documents to ensure there are no errors. Make sure your application is complete and includes all required documents as specified in the job listing.
How to prepare for a job interview at AstraZeneca
✨Show Your Passion for Science
Make sure to express your enthusiasm for science and how it drives you to make a difference in patients' lives. Share specific examples of how your passion has influenced your work in clinical research.
✨Demonstrate Project Management Skills
Be prepared to discuss your project management experience in detail. Highlight specific tools and methodologies you've used, and how they contributed to the successful delivery of clinical studies.
✨Familiarize Yourself with GCP and Regulatory Requirements
Brush up on Good Clinical Practice (GCP) guidelines and relevant regulatory requirements. Be ready to discuss how you have applied this knowledge in your previous roles to ensure compliance and quality in study management.
✨Prepare for Cross-Functional Collaboration Questions
Expect questions about your experience working with cross-functional teams. Prepare examples that showcase your ability to facilitate communication and collaboration between different stakeholders, such as internal teams and external partners.
